Recurrent European missense mutation in the <i>F12</i> gene in a British family with type III hereditary angioedema期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

*Recurrent European missense mutation in the F12* gene in a British family with type III hereditary angioedema**

Authors:	Nikoletta Nagy Malcolm W. Greaves Akio Tanaka John A. McGrath Clive E. Grattan

Affiliation:	^aSt John's Institute of Dermatology, King's College London, Guy's Campus, London, UK;^bDepartment of Dermatology, Poole General Hospital, Poole, Dorset, UK;^cSt John's Institute of Dermatology, The Guy's and St Thomas’ NHS Foundation Trust, London, UK;^dDepartment of Dermatology, Norfolk and Norwich University Hospital, Norwich, UK

Abstract:

Keywords:	Bradykinin Coagulation factor XII Oedema Skin Genetic disease
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